Canonical Allele Identifier: CA1565024403
Gene: SKIC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.95516682T= , CM000667.2:g.95516682T= GRCh38
NC_000005.9:g.94852386T= , CM000667.1:g.94852386T= GRCh37
NC_000005.8:g.94878142T= NCBI36
NG_023414.1:g.43324A= , LRG_173:g.43324A=

Transcript Alleles

HGVS Amino-acid change
ENST00000506007.2:n.2960A=
ENST00000513232.2:c.*1385A= ENSP00000422749.2:n.*1385A=
ENST00000698450.1:n.1889A=
ENST00000698451.1:n.2090A=
ENST00000698452.1:n.3161A=
ENST00000698453.1:c.2442-96A= ENSP00000513735.1:n.2442-96A=
ENST00000698454.1:c.2496A= ENSP00000513736.1:p.Ala832=
ENST00000698455.1:c.*2646A= ENSP00000513737.1:n.*2646A=
ENST00000698456.1:c.*1363A= ENSP00000513738.1:n.*1363A=
ENST00000698457.1:c.2295A= ENSP00000513739.1:p.Ala765=
ENST00000698458.1:c.2478-96A= ENSP00000513740.1:n.2478-96A=
ENST00000698459.1:c.2505A= ENSP00000513741.1:p.Ala835=
ENST00000698460.1:c.*279-96A= ENSP00000513742.1:n.*279-96A=
ENST00000698461.1:n.2960A=
ENST00000698462.1:n.2880A=
ENST00000698468.1:n.3161A=
ENST00000698469.1:c.*2017A= ENSP00000513743.1:n.*2017A=
ENST00000698470.1:c.*512A= ENSP00000513744.1:n.*512A=
ENST00000698471.1:n.2960A=
ENST00000698472.1:c.*1385A= ENSP00000513745.1:n.*1385A=
ENST00000698473.1:n.2960A=
ENST00000698474.1:n.2960A=
ENST00000698475.1:n.3045A=
ENST00000698476.1:c.2505A= ENSP00000513746.1:p.Ala835=
ENST00000698477.1:c.2442-96A= ENSP00000513747.1:n.2442-96A=
ENST00000698478.1:n.2960A=
ENST00000698479.1:c.2505A= ENSP00000513748.1:p.Ala835=
ENST00000698480.1:c.2437-96A= ENSP00000513749.1:n.2437-96A=
ENST00000698481.1:c.2437-96A= ENSP00000513750.1:n.2437-96A=
ENST00000698482.1:n.2795A=
ENST00000698483.1:n.2960A=
ENST00000698484.1:c.2505A= ENSP00000513751.1:p.Ala835=
ENST00000698485.1:c.2437-96A= ENSP00000513752.1:n.2437-96A=
ENST00000698486.1:n.2960A=
ENST00000698487.1:c.2505A= ENSP00000513753.1:p.Ala835=
ENST00000698488.1:c.2260-96A= ENSP00000513754.1:n.2260-96A=
ENST00000698489.1:n.6745A=
ENST00000698490.1:c.2505A= ENSP00000513755.1:p.Ala835=
ENST00000698492.1:c.*1220A= ENSP00000513756.1:n.*1220A=
ENST00000698493.1:n.2795A=
ENST00000698494.1:c.*400A= ENSP00000513757.1:n.*400A=
ENST00000358746.7:c.2505A= MANE Select ENSP00000351596.3:p.Ala835=
ENST00000649566.1:c.2505A= ENSP00000497948.1:p.Ala835=
ENST00000358746.6:c.2505A= ENSP00000351596.2:p.Ala835=
ENST00000506007.1:n.87A=
ENST00000507805.5:n.692A=
NM_014639.3:c.2505A= , LRG_173t1:c.2505A= NP_055454.1:p.Ala835=
XR_948312.1:n.2774A=
XR_001742370.2:n.2777A=
NM_014639.4:c.2505A= MANE Select NP_055454.1:p.Ala835=